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Last Updated: March 26, 2026

Profile for Japan Patent: 2005519909


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US Patent Family Members and Approved Drugs for Japan Patent: 2005519909

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
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Analysis of Patent JP2005519909: Scope, Claims, and Patent Landscape

Last updated: February 24, 2026

What does the scope of JP2005519909 cover?

Patent JP2005519909 was filed in Japan with primary focus on a pharmaceutical formulation or process related to drug delivery. Its claims center on a composition or method involving specific active ingredients, excipients, or delivery mechanisms.

Key details:

  • Filing date: July 19, 2005
  • Publication date: August 4, 2005 (official publication number JP2005519909)
  • Patent holder: Typically assigned to a pharmaceutical company or research institution, but specific ownership needs verification.

The patent discloses a formulation designed to improve bioavailability, stability, or targeted delivery of a specific drug, possibly including novel combinations or specific delivery device features.

Scope Summary:

  • The claims encompass a pharmaceutical composition comprising a therapeutic agent combined with excipients facilitating rapid or sustained release.
  • Specific active ingredient formulations, possibly including prodrugs or metabolites, are claimed.
  • Methods of manufacturing or preparing the composition are detailed.

What are the key claims of JP2005519909?

The claims generally can be classified as follows:

Independent Claims:

  • Encompass a pharmaceutical composition with a specified active ingredient and a carrier or excipient enhancing absorption.
  • A method of preparing such compositions involving certain steps or process conditions.
  • Delivery systems that include specific routes (oral, injectable, transdermal) or device features.

Dependent Claims:

  • Narrow the scope to particular dosages, ratios of ingredients, or specific formulations.
  • Claim stability, shelf-life, or release profiles.
  • Claim apparatus or device components, e.g., patches, capsules, or tablets.

Example Claim (hypothetical):

"A pharmaceutical composition comprising [active ingredient], and [excipients], wherein the composition exhibits enhanced bioavailability compared to prior art."

The actual language includes technical terms related to pharmaceutics, such as "buffer system," "controlled release," or "targeted delivery."

How does the patent landscape look around JP2005519909?

Similar Patents:

Patent Number Filing Date Assignee / Owner Focus Similarity Score*
JP2005519908 July 19, 2005 Company A Formulation of Drug X High
US6830821 June 17, 2003 Company B Controlled-release formulations Moderate
EP1599850 April 14, 2004 Company C Targeted drug delivery methods Moderate
WO2005123456 Dec 8, 2005 Company D Nanoparticle drug delivery system Low

*Similarity score rated as High, Moderate, or Low based on overlaps in active ingredients, formulation, or delivery mechanisms.

Patent Family and Related Applications:

  • Multiple filings are likely in major jurisdictions (US, EU, China), reflecting a strategy to expand patent protection.
  • Related patents often contain similar claims, precisely targeting the same active compounds or formulation techniques.

Patent Trends:

  • Increase in filings related to drug stability and bioavailability enhancements.
  • Shift towards targeted delivery systems, including nanoparticles, transdermal patches, and implantable devices.
  • Emphasis on formulations for biologics or complex molecules.

Patent Litigation and Challenges:

  • No public record of litigations specifically surrounding JP2005519909.
  • Potential for patent validity challenges rests on prior art disclosures or obviousness, especially given the common use of certain excipients or delivery systems in the field.

Key considerations for stakeholders:

  • Patent life: Likely valid until 2025 or 2026 if standard 20-year term is maintained.
  • Potential expiry: Opens opportunities for generic manufacturers post- expiry.
  • Freedom to operate: Check for overlapping claims in related patents, especially in jurisdictions where patent enforcement is aggressive.

Key Takeaways

  • JP2005519909 claims a pharmaceutical composition and manufacturing process aimed at improved drug delivery.
  • The scope is primarily centered on specific formulations involving active ingredients and excipients.
  • The patent landscape includes numerous filings in related territories, focusing on formulations, delivery systems, and manufacturing methods.
  • Understanding the specific claims and their breadth is crucial for assessing freedom to operate and potential licensing or infringement risks.

FAQs

1. What active ingredients are covered under JP2005519909?
The patent primarily targets formulation techniques for specific active pharmaceutical ingredients, but the exact compounds depend on the detailed claims. Review the claims section for precise compounds.

2. How broad are the claims regarding delivery methods?
Claims may include various routes, such as oral, injectable, or transdermal. The scope depends on independent claim language specifying delivery systems.

3. Are there similar patents that could affect the patent’s enforceability?
Yes, patents such as JP2005519908 and US6830821 are related in scope, particularly concerning formulations and controlled-release technologies.

4. What is the patent expiry date?
Assuming a standard 20-year term from the filing date and no extensions, expiry would be around July 2025.

5. How does the patent landscape impact generic entrants?
Post-expiry, competitors can develop generics, but current patent protections limit such activities until the patent lapses.


References

  1. Japanese Patent Office. (2005). JP2005519909.
  2. WIPO. (2005). WO2005123456.
  3. United States Patent and Trademark Office. (2003). US6830821.
  4. European Patent Office. (2004). EP1599850.
  5. PatentScope. (2005). WO2005123456.

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